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Latex binders, aqueous coatings and paints having freeze-thaw ability and methods for using same

a technology of which is applied in the field of latex binders, aqueous coatings and paints having freeze-thaw ability and methods for using same, can solve the problems that particles with relatively low tg cannot recover from aggregation or coalescence states, and achieve the effect of improving freeze-thaw stability and being easy to recover

Active Publication Date: 2009-07-23
RHODIA OPERATIONS SAS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0014]The present invention relates to the use of a particular family of alkoxylated compounds with bulky hydrophobic groups, e.g., alkoxylated tristyrylphenols or alkoxylated tributylphenols, for improving freeze-thaw stability, as well as other properties such as open time, low temperature film formation, stain resistance, film gloss, dispersibility, hiding and scrub resistance, foam resistance, block resistance, adhesion and water sensitivity, among others, of latex binders, paints and coatings. During the thawing process of the freeze-thaw process in latex dispersions and paint formulation, it is believed that the latex particles with high Tg are easy to recover, while the particles with relatively low Tg can not recover from the aggregation or coalescence states which gel.
[0015]While not being bound to theory, it is theorized the present invention in part stabilizes the latex particles using steric effects of larger hydrophobic groups to form a protective layer on the surfaces of soft latex particles. The large hydrophobic groups adsorbed or grafted onto the latex particles or co-polymerized into the latex particles prevent these latex particles from approaching the surfaces of other soft latex particles and increase the distance of separation between soft latex particles. The alkylene, e.g., ethylene oxide units from the surfactant of the alkoxylated compounds chains also form a layer which interacts with aqueous medium.
[0017]The alkoxylated compounds can be employed in a number of ways for improving freeze-thaw stability of latex binders, paints and coatings. The present invention may employ polymerizable reactive alkoxylated monomers as a reactant during emulsion polymerization to form the latex polymer. The present invention may employ one or more surface active alkoxylated compounds described herein as a surfactant (emulsifier) during emulsion polymerization to form the latex polymer. The present invention may employ a surface active alkoxylated compound as an additive to a latex polymer-containing aqueous dispersion or concentrate.
[0028]In a further embodiment, the composition of the present invention is freeze-thaw stable, and the polymer can have a Tg of between about −15° C. and about 12° C. and a mean particle size of less than about 200 nm, or a Tg of between about −5° C. and about 5° C. and a mean particle size of less than about 200 nm, or a Tg of between about −5° C. and about 0° C. and a mean particle size of less than about 200 nm, or a Tg of between about −15° C. and about 12° C. and a mean particle size of less than about 190 nm, or a Tg of between about −5° C. and about 5° C. and a mean particle size of less than about 190 nm, or a Tg of between about −5° C. and about 0° C. and a mean particle size of less than about 190 nm, or a Tg of between about −15° C. and about 12° C. and a mean particle size of less than about 175 nm, or a Tg of between about −5° C. and about 5° C. and a mean particle size of less than about 175 nm, or a Tg of between about −5° C. and about 0° C. and a mean particle size of less than about 175 nm.

Problems solved by technology

During the thawing process of the freeze-thaw process in latex dispersions and paint formulation, it is believed that the latex particles with high Tg are easy to recover, while the particles with relatively low Tg can not recover from the aggregation or coalescence states which gel.

Method used

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  • Latex binders, aqueous coatings and paints having freeze-thaw ability and methods for using same
  • Latex binders, aqueous coatings and paints having freeze-thaw ability and methods for using same
  • Latex binders, aqueous coatings and paints having freeze-thaw ability and methods for using same

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0160]Freeze Thaw Stability Study—Example 1 compares a control with compositions of the present invention, which incorporate various levels of TSP-EO and 1% MM (methacrylic acid). TSP-EO is a surface active ethoxylated tristyrylphenol according to the above-listed structural formula IIC in which the R group is H.

[0161]Sample 1 of the present invention with 2% TSP-EO, 1% MM (methacrylic acid); Sample 2 of the present invention with 4% TSP-EO, 1% MM; and Sample 3 of the present invention with 6% TSP-EO, 1% MM were made. TABLE 1 shows the ingredients of Sample 2 which is an embodiment of the present invention with 4% TSP-EO, 1% MM.

TABLE 1SAMPLE 2 INGREDIENTSIngredient weightRecipe:(grams)% BOTMKettle ChargeDeionized Water200.00Monomer EmulsionDeionized Water176.25Alkyl sulfate surfactant18.751.50Non-ionic surfactant5.000.50TSP - EO20.004.00Methylmethacrylate (MMA)200.0040.00butylacrylate (BA)295.0059.00(methyl acrylic acid) MAA5.001.00Initiator SolutionDeionized Water98.00Ammonium Pers...

example 1-1

[0176]The above-described procedure was repeated with a variety of anionic or nonionic ethoxylated tristerylphenolic (TSP) compounds having from about 6 ethylene oxide groups to about 60 ethylene oxide groups. TABLE 4 presents the results of these examples.

TABLE 4Effects of Additives on Freeze-Thaw Stability of Water-Borne Paints2Freeze-Thaw StabilityViscosity (KU)1Starting2345AdditivesViscosity1 cyclecyclescyclescyclescyclesTSP-EO #1102.4103.8104.3104104105.4TSP-EO #298.3101.9102.2101.2100.2101.3TSP-EO #382.986.688.889.490.491.5TSP-EO #47888.390.291.693.3101.4TSP-EO #578.48286.48685.487.1TSP-EO #680.891.995.196.296.597.6Ethoxylated95.5Failednonylphenol3(gelled)Control121.1Failed(Low VOC(gelled)CommercialPaint)Notes:1Additive loading level: 1.0 Wt % of total paint weight.2Water-borne commercial paint: Weight per Gallon: 10.24 pounds per gallon; pH: 8.67; VOC: 3Nonylphenol moiety attached to 9EO

[0177]Example 2 illustrates comparative examples of the present invention as against the d...

example 2

[0178]The seed latex according to the '512 application (p. 20) was prepared:

[0179]Seed Latex Preparation using Sodium Lauryl Sulfate (SLS)

Formulas:Water50Sulfate*: (29.5)2.44Monomers:Styrene7.2MMA12.24BA15.84AA0.72Total100Initiator SolutionAmmonium Persulfate0.26Water14

[0180]Procedure: 1. Add 150 water and 7.32 g surfactant (SLS) to the kettle and heat to ˜83° C. 2. Add 42.78 g initiator solution. 3. Add 108 monomer mixture to kettle and hold at ˜83° C. over 2-3 hours. 4. Measure the particle size during emulsion polymerization process. 5. Cool to room temperature and keep the seed latex for future usage. The active wt % of the seed latex was 36 wt %.

[0181]Tables 5 and 6 illustrate emulsion polymerization of a styrene-acrylic latex polymer using SLS (control) and using SLS in combination with a TSP having from about 10 to 40 ethylene oxide groups as surfactant emulsifiers, respectively.

TABLE 5Styrene-Acrylic Latex Polymer - Sodium Lauryl Sulfate (Control)Recipe:Ingredient weight (g)...

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Abstract

Disclosed are latex polymers and an aqueous coating compositions having excellent freeze-thaw stability, open time, stain resistance, low temperature film formation, foam resistance, block resistance, adhesion, water sensitivity and a low-VOC content. The latex polymers and aqueous coating compositions include at least one latex polymer derived from at least one monomer copolymerized or blended with an alkoxylated compound, for example an alkoxylated tristyrylphenol or an alkoxylated tributylphenol. Also provided is an aqueous coating composition including at least one latex polymer, at least one pigment, water and at least one freeze-thaw additive. Typically, the freeze-thaw additive in an amount greater than about 1.3% by weight of the polymer, typically in an amount greater than about 2% by weight of the polymer, in an amount greater than about 4% by weight of the polymer, in an amount greater than about 7.5% by weight of the polymer, in an amount greater than about 10% by weight of the polymer or in an amount greater than about 20% by weight of the polymer.

Description

CROSS REFERENCE TO RELATED APPLICATIONS[0001]This application claims the benefit of U.S. Provisional Application Ser. No. 61 / 022,206, filed Jan. 18, 2008, U.S. Provisional Application Ser. No. 61 / 022,443, filed Jan. 21, 2008 and U.S. Provisional Application Ser. No. 61 / 199,936, filed Nov. 21, 2008, all herein incorporated by referenceFIELD OF THE INVENTION[0002]The present invention relates to the use of a particular family of alkoxylated compounds, e.g alkoxylated tristyrylphenol and alkoxylated tributylphenol, for improving freeze-thaw stability and open time of aqueous coating compositions such as paint and paper coating compositions. In particular, the present invention relates to the use of certain reactive alkoxylated compound based monomers, surface active alkoxylated compound surfactants, and surface active alkoxylated compound additives for freeze-thaw stability of aqueous latex dispersions, aqueous latex binders and aqueous latex paints.BACKGROUND OF THE INVENTION[0003]Lat...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C08K5/5333C08F12/24C08L33/08C08K5/06C08K5/521C08K5/41B32B5/02
CPCC07C43/23C08K5/0008C09D133/02C08F212/08C08L25/16Y10T428/2982C08F2/24C09D125/14C09D125/16C08L25/14C08F220/30C09D133/08C08F220/1804C08F220/14C08F220/06C07C41/05C08F20/00C08K5/00C09D5/02
Inventor ZONG, ZHENGANGLI, YI-ZHONGRUIZ, JOSE
Owner RHODIA OPERATIONS SAS
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